ASSEMBLY OF 2-D MEMBRANE-PROTEIN CRYSTALS - DYNAMICS, CRYSTAL ORDER, AND FIDELITY OF STRUCTURE-ANALYSIS BY ELECTRON-MICROSCOPY

被引:59
|
作者
ENGEL, A
HOENGER, A
HEFTI, A
HENN, C
FORD, RC
KISTLER, J
ZULAUF, M
机构
[1] UNIV MANCHESTER, INST SCI & TECHNOL, DEPT BIOCHEM & APPL MOLEC BIOL, MANCHESTER M60 1QD, LANCS, ENGLAND
[2] UNIV AUCKLAND, CTR GENE TECHNOL, DEPT CELLULAR & MOLEC BIOL, AUCKLAND, NEW ZEALAND
[3] F HOFFMANN LA ROCHE & CO LTD, PHARMA RES NEW TECHNOL, CH-4002 BASEL, SWITZERLAND
关键词
D O I
10.1016/1047-8477(92)90035-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane protein reconstitution into two-dimensional (2-D) ordered arrays is described. The assembly of 2-D crystals may be modeled as a two-step process: the membrane protein is first integrated in the lipid bilayer and then crystallized by removal of excess detergent or lipid and/or by precipitating agents. Lipid-detergent, protein-detergent, and lipid-protein interactions are critical during the first step, while lipid-protein and protein-protein interactions dominate events in the second step. The evidence supporting this model results from quasielastic light scattering analyses and electron microscopy of different lipid-detergent systems and reconstitution experiments with Escherichia coli porin OmpF, Phormidium laminosum photosystem I reaction centers, and integral membrane proteins of mammalian lens fiber cells. © 1992.
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页码:219 / 234
页数:16
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